United States · FDA National Drug Code directory

Hand Sanitizer

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
70412-191_098716b8-14a3-8ab4-e063-6394a90a2bc8
Product NDC
70412-191
Form
GEL
Composition / generic term
ALCOHOL
Labeler
Zhejiang Ayan Biotech Co.,Ltd.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20200420
Source listing expiry
20261231

Source-listed ingredients

  • ALCOHOL — .62 mL/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 236 mL in 1 BOTTLE (70412-191-08) · 70412-191-08
  • 473 mL in 1 BOTTLE (70412-191-16) · 70412-191-16

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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